Description

Azilsartan is a potent and selective angiotensin II receptor blocker (ARB) used as an active pharmaceutical ingredient (API). It is a key therapeutic agent in the management of hypertension, offering effective blood pressure control. This high-purity compound is essential for pharmaceutical manufacturers developing finished dosage forms, such as tablets, for the global cardiovascular drug market.

Application

• Pharmaceutical API: Primary use as the active ingredient in antihypertensive medications.
• Finished Dosage Formulation: Direct compression into tablets, often in combination with other antihypertensives like chlorthalidone.
• Cardiovascular Research: Used in preclinical and clinical studies for investigating new hypertension treatments.
• Reference Standard: Serves as a high-purity analytical standard for quality control testing in pharmaceutical labs.
• Generic Drug Manufacturing: Critical for producing bioequivalent generic versions of branded azilsartan medications.

Basic Information

Product Name	Azilsartan
CAS No.	147403-03-0
Molecular Formula	C25H20N4O5
Molecular Weight	456.45 g/mol
Synonyms	Azilsartan Kamedoxomil; TAK-491 (Free Acid); 2-Ethoxy-1-[[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylic Acid; (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 2-ethoxy-1-[[2'-(5-oxo-4H-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate (Kamedoxomil Ester); TAK-536; Edarbi (Brand Name API)
EINECS	Contact for details

Quality Control

Our Azilsartan is manufactured under strict quality management systems. It is produced to meet or exceed pharmaceutical-grade specifications, including relevant ICH guidelines. Comprehensive testing is performed to ensure identity, purity, and potency. A Certificate of Analysis (COA) detailing all test results is provided with each batch to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); ensure the container is kept tightly sealed in a low-humidity environment to maintain stability and prevent degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 1.0%; Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.